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In a conventional molecular cloning experiment, the DNA to be cloned is obtained from an organism of interest, then treated with enzymes in the test tube to generate smaller DNA fragments. Subsequently, these fragments are then combined with vector DNA to generate recombinant DNA molecules. The recombinant DNA is then introduced into a host organism (typically an easy-to-grow, benign, laboratory strain of E. coli bacteria). This will generate a population of organisms in which recombinant DNA molecules are replicated along with the host DNA. Because they contain foreign DNA fragments, these are transgenic or genetically modified microorganisms (GMO).This process takes advantage of the fact that a single bacterial cell can be induced to take up and replicate a single
Young Research Forum: Journal of Glycobiology
Research Article: Journal of Glycobiology
Research Article: Journal of Glycobiology
Research Article: Journal of Glycobiology
Research Article: Journal of Glycobiology
Posters-Accepted Abstracts: Journal of Chromatography & Separation Techniques
Posters & Accepted Abstracts: Journal of Chemical Engineering & Process Technology
Keynote: Journal of Glycobiology